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Variant : CV593198 (GRCh37/hg19 14q23.1(chr14:58666970-59006831)x3) Homo sapiens

Symbol: CV593198
Name: GRCh37/hg19 14q23.1(chr14:58666970-59006831)x3
Condition: not provided [RCV000738498]
Clinical Significance: benign
Last Evaluated: 03/13/2013
Review Status: no assertion criteria provided
Related Genes: ACTR10   ARID4A   KIAA0586   PSMA3   TIMM9   TOMM20L  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371458,666,970 - 59,006,831CLINVAR
Cytogenetic Map1414q23.1CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14353878
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.